{[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane

Base Information

Chemical Name:{[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane
CAS No.:856687-75-7
Molecular Formula:C₂₇H₄₁IO₃Si
Molecular Weight:568.611
Hs Code.:

Synonyms:{[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane

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Chemical Property of {[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane

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Technology Process of {[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane

There total 6 articles about {[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 856687-73-5
(2S)-2-[(S)-(3,5-dimethoxy-4-methylphenyl){[dimethyl(2-methyl-2-propanyl)silyl]oxy}methyl]-5-phenylpentyl methanesulfonate

: 856687-75-7
{[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane

Guidance literature:: With sodium iodide; In acetone; at 90 ℃; for 3h;

Reference yield:

: 1011-27-4
3,5-dimethoxy-4-methylbenzaldehyde

: 856687-75-7
{[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine; chloro-trimethyl-silane; magnesium chloride / ethyl acetate / 20 °C

1.2: 0.08 h

2.1: 2,6-dimethylpyridine / dichloromethane / 2 h / 0 °C

3.1: lithium borohydride / tetrahydrofuran; water / 3 h / 0 - 20 °C / Inert atmosphere

4.1: triethylamine / tetrahydrofuran / 0.25 h / 0 - 20 °C

5.1: sodium iodide / acetone / 3 h / 90 °C

With 2,6-dimethylpyridine; lithium borohydride; chloro-trimethyl-silane; triethylamine; sodium iodide; magnesium chloride; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetone;
DOI:10.1021/acsmedchemlett.7b00383

Reference yield:

: 161725-13-9
(4S)-4-benzyl-3-(5-phenylpentanoyl)-1,3-oxazolidin-2-one

: 856687-75-7
{[(1S,2R)-1-(3,5-dimethoxy-4-methylphenyl)-2-(iodomethyl)-5-phenylpentyl]oxy}(dimethyl)(2-methyl-2-propanyl)silane

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine; chloro-trimethyl-silane; magnesium chloride / ethyl acetate / 20 °C

1.2: 0.08 h

2.1: 2,6-dimethylpyridine / dichloromethane / 2 h / 0 °C

3.1: lithium borohydride / tetrahydrofuran; water / 3 h / 0 - 20 °C / Inert atmosphere

4.1: triethylamine / tetrahydrofuran / 0.25 h / 0 - 20 °C

5.1: sodium iodide / acetone / 3 h / 90 °C

With 2,6-dimethylpyridine; lithium borohydride; chloro-trimethyl-silane; triethylamine; sodium iodide; magnesium chloride; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetone;
DOI:10.1021/acsmedchemlett.7b00383